Peripheral blood molecular measurable residual disease is sufficient to identify patients with acute myeloid leukaemia with imminent clinical relapse

Anne Sofie Skou, Kristian Løvvik Juul-Dam, Hans B. Ommen, Henrik Hasle*

*Corresponding author for this work

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperReviewResearchpeer-review

11 Citations (Scopus)

Abstract

Longitudinal molecular measurable residual disease (MRD) sampling after completion of therapy serves as a refined tool for identification of imminent relapse of acute myeloid leukaemia (AML) among patients in long-term haematological complete remission. Tracking of increasing quantitative polymerase chain reaction MRD before cytomorphological reappearance of blasts may instigate individual management decisions and has paved the way for development of pre-emptive treatment strategies to substantially delay or perhaps even revert leukaemic regrowth. Traditionally, MRD monitoring is performed using repeated bone marrow aspirations, albeit the current European LeukemiaNet MRD recommendations acknowledge the use of peripheral blood as an alternative source for MRD assessment. Persistent MRD positivity in the bone marrow despite continuous morphological remission is frequent in both core binding factor leukaemias and nucleophosmin 1-mutated AML. In contrast, monthly assessment of MRD in peripheral blood superiorly separates patients with imminent haematological relapse from long-term remitters and may allow pre-emptive therapy of AML relapse.

Original languageEnglish
JournalBritish Journal of Haematology
Volume195
Issue3
Pages (from-to)310-327
Number of pages18
ISSN0007-1048
DOIs
Publication statusPublished - Nov 2021

Keywords

  • acute myeloid leukaemia
  • measurable residual disease
  • molecular relapse
  • pre-emptive therapy
  • quantitative polymerase chain reaction

Fingerprint

Dive into the research topics of 'Peripheral blood molecular measurable residual disease is sufficient to identify patients with acute myeloid leukaemia with imminent clinical relapse'. Together they form a unique fingerprint.

Cite this